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Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits

Urotensin II (UII) is a vasoactive peptide composed of 11 amino acids that has been implicated to contribute to the development of cardiovascular disease. The purpose of this study was to investigate whether UII affects the development of atherosclerosis in cholesterol-fed rabbits. UII was infused f...

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Autores principales: Li, Yafeng, Zhao, Sihai, Wang, Yanli, Chen, Yulong, Lin, Yan, Zhu, Ninghong, Zheng, Huadong, Wu, Min, Cheng, Daxing, Li, Yandong, Bai, Liang, Fan, Jianglin, Liu, Enqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991611/
https://www.ncbi.nlm.nih.gov/pubmed/24747943
http://dx.doi.org/10.1371/journal.pone.0095089
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author Li, Yafeng
Zhao, Sihai
Wang, Yanli
Chen, Yulong
Lin, Yan
Zhu, Ninghong
Zheng, Huadong
Wu, Min
Cheng, Daxing
Li, Yandong
Bai, Liang
Fan, Jianglin
Liu, Enqi
author_facet Li, Yafeng
Zhao, Sihai
Wang, Yanli
Chen, Yulong
Lin, Yan
Zhu, Ninghong
Zheng, Huadong
Wu, Min
Cheng, Daxing
Li, Yandong
Bai, Liang
Fan, Jianglin
Liu, Enqi
author_sort Li, Yafeng
collection PubMed
description Urotensin II (UII) is a vasoactive peptide composed of 11 amino acids that has been implicated to contribute to the development of cardiovascular disease. The purpose of this study was to investigate whether UII affects the development of atherosclerosis in cholesterol-fed rabbits. UII was infused for 16 weeks through an osmotic mini-pump into male Japanese White rabbits fed on a high-cholesterol diet. Plasma lipids and body weight were measured every 4 weeks. Aortic atherosclerotic lesions along with cellular components, collagen fibers, matrix metalloproteinase-1 and -9 were examined. Moreover, vulnerability index of atherosclerotic plaques was evaluated. UII infusion significantly increased atherosclerotic lesions within the entire aorta by 21% over the control (P = 0.013). Atherosclerotic lesions were increased by 24% in the aortic arch (P = 0.005), 11% in the thoracic aorta (P = 0.054) and 18% in the abdominal aorta (P = 0.035). These increases occurred without changes in plasma levels of total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides or body weight. Immunohistochemical staining revealed that macrophages and matrix metalloproteinase-9 were significantly enhanced by 2.2-fold and 1.6-fold in UII group. In vitro studies demonstrated that UII up-regulated the expression of vascular cell adhesion protein-1 and intercellular adhesion molecule-1 in human umbilical vein endothelial cells, which was inhibited by the UII receptor antagonist urantide. In conclusion, our results showed that UII promotes the development of atherosclerotic lesions and destabilizes atherosclerotic plaques in cholesterol-fed rabbits.
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spelling pubmed-39916112014-04-21 Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits Li, Yafeng Zhao, Sihai Wang, Yanli Chen, Yulong Lin, Yan Zhu, Ninghong Zheng, Huadong Wu, Min Cheng, Daxing Li, Yandong Bai, Liang Fan, Jianglin Liu, Enqi PLoS One Research Article Urotensin II (UII) is a vasoactive peptide composed of 11 amino acids that has been implicated to contribute to the development of cardiovascular disease. The purpose of this study was to investigate whether UII affects the development of atherosclerosis in cholesterol-fed rabbits. UII was infused for 16 weeks through an osmotic mini-pump into male Japanese White rabbits fed on a high-cholesterol diet. Plasma lipids and body weight were measured every 4 weeks. Aortic atherosclerotic lesions along with cellular components, collagen fibers, matrix metalloproteinase-1 and -9 were examined. Moreover, vulnerability index of atherosclerotic plaques was evaluated. UII infusion significantly increased atherosclerotic lesions within the entire aorta by 21% over the control (P = 0.013). Atherosclerotic lesions were increased by 24% in the aortic arch (P = 0.005), 11% in the thoracic aorta (P = 0.054) and 18% in the abdominal aorta (P = 0.035). These increases occurred without changes in plasma levels of total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides or body weight. Immunohistochemical staining revealed that macrophages and matrix metalloproteinase-9 were significantly enhanced by 2.2-fold and 1.6-fold in UII group. In vitro studies demonstrated that UII up-regulated the expression of vascular cell adhesion protein-1 and intercellular adhesion molecule-1 in human umbilical vein endothelial cells, which was inhibited by the UII receptor antagonist urantide. In conclusion, our results showed that UII promotes the development of atherosclerotic lesions and destabilizes atherosclerotic plaques in cholesterol-fed rabbits. Public Library of Science 2014-04-18 /pmc/articles/PMC3991611/ /pubmed/24747943 http://dx.doi.org/10.1371/journal.pone.0095089 Text en © 2014 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Yafeng
Zhao, Sihai
Wang, Yanli
Chen, Yulong
Lin, Yan
Zhu, Ninghong
Zheng, Huadong
Wu, Min
Cheng, Daxing
Li, Yandong
Bai, Liang
Fan, Jianglin
Liu, Enqi
Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title_full Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title_fullStr Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title_full_unstemmed Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title_short Urotensin II Promotes Atherosclerosis in Cholesterol-Fed Rabbits
title_sort urotensin ii promotes atherosclerosis in cholesterol-fed rabbits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3991611/
https://www.ncbi.nlm.nih.gov/pubmed/24747943
http://dx.doi.org/10.1371/journal.pone.0095089
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